维普期刊资源整合服务平台（V6.5）

107篇 您的检索式：期刊名="J HumGenet"

选中清除导出查看参考文献查看引证文献引用追踪共6页首页上一页第1页下一页末页 /6 跳转

	题名	作者	年代	出处	被引量
1	Linkage of autosomal recessive lamellar ichthyosis to chromosome 14q 显示文摘	RUSSELL L J DIGIOVANNA J J HASHEM N	1994	Am J HumGenet1994，55，：	1
2	Accumulation of mitochondrialDNA mutations in human immunodeficiency virus-infected patients treatedwith nucleoside-analogue reverse-transcriptase inhibitors显示文摘	Martin AM Hammond E Nolan D	2003	Am J HumGenet2003，72，3：	1
3	Construction of a genetic link- agemap in man using restriction fragment length polymor- phisms显示文摘	Botstein D White R L	1980	Am J HumGenet1980，32，：	1
4	Strategies for the rapidprenatal diagnosis of chromosome aneuploidy显示文摘	Mann K Donaghue C Fox S P	2004	Eur J HumGenet2004，12，11：	1
5	Linkage of autosomal recessive lamellar ichyosis to chromosome 14q 显示文摘	Dogiovanna JJ Hashem N	1994	Am J HumGenet1994，55，6：	1
6	Association of a polymorphism at the 5'region of the angiotensin Ⅱ type 1 receptor with hypertension显示文摘	Takahashi N Hurakami H	2000	J Ann HumGenet2000，64，：	1
7	Mutation profile of all 49 exons of the humann MyosinVIIA gene and haplotype analysis in Usher IB families from diverse origins显示文摘	7,Adato A Weil D Halinski H	1997	Am J HumGenet1997，61，：	1
8	A common haplotype of the nicotine acetylcholine receptor alpha 4 subunit gene is associated with vulnerability to nicotine addiction in men显示文摘	Feng Y Niu T Xing H	2004	Am J HumGenet2004，75，：	1
9	Association of Adam33 gene polymorphisms with asthma in Indian children 显示文摘	Awasthi S Tripathi P Ganesh S	2011	J HumGenet2011，56，3：	1
10	Paget's disease (osteitis deformans) and he- reditary显示文摘	Montagu MFA	1949	Am J HumGenet1949，1，：	1
11	Analysis offour neuroligin genes as candidates for autism显示文摘	Ylisaukko-oja T Rehnstrom K Auranen M	2005	Eur J HumGenet2005，13，12：	1
12	Pharmacogenetic determinants ofvariability in lipid-lowering response to pravastatin therapy显示文摘	Takane H Miyata M Burioka N	2006	J HumGenet2006，51，：	1
13	Methylation analysis of the intergenic differentially methylated region of DLKI-GTL2 in human显示文摘	De Temmerman N Hilven P	2007	Eur J HumGenet2007，15，3：	1
14	The human EZH2 gene:genomic organisation and revised mapping in 7q35 within thecritical region for malignant myeloid disorders显示文摘	Cardoso C Mignon C Hetet G	2000	Eur J HumGenet2000，8，3：	1
15	Transmission of mtDNA: cracks in the bottleneck 显示文摘	Poulton J	1995	Am J HumGenet1995，57，2：	1
16	Insertion and dele-tion mutations in the dinucleotide repeat region of the Norrie diseasegene in patients with advanced retinopathy of prematurity 显示文摘	Hiraoka M Berinstein DM Trese MX	2001	J HumGenet2001，46，4：	1
17	A syndactyly type Ⅳ locus maps to 7q36显示文摘	Sato D Liang D Wu L	2007	J HumGenet2007，52，6：	1
18	Confirmation of thetype 2myotonic dystrophy(CCTG)n expansion mutation inpatients with proximal myotonic myopathy/proximal myoton-ic dystrophy of different European origins:a single sharedhaplotype indicates an ancestral founder effect显示文摘	Bachinski LL Udd B Meola G	2003	Am J HumGenet2003，73，4：	1
19	Towards mapping phenotypical traits in 18p-syndrome by array-based comparative genomic hybridisation and fluorescent in situ hybridisation显示文摘	Brenk CH Prott EC Trost D	2007	Eur J HumGenet2007，15，1：	1
20	Structure of The chromosomal gene and cDNAs coding for lctase phlorizinhydrolasein humans with adult-type hypolactasiaor persistence of lactase 显示文摘	BollW WaguerP ManteiN	1991	Am J HumGenet1991，48，：	1

返回顶部每页显示：

共6页首页上一页第1页下一页末页 /6 跳转

互联网出版许可证新出网证(渝)字10号全国400电话 - 免长途话费

用户提示